Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43358674-43359009 | Common:7; Rare:104 | ||||
chr1:43367965-43368212 | Rare:67 | ||||
chr1:43389786-43389926 | Common:3; Rare:50 | ||||
chr1:43707333-43707562 | Common:2; Rare:67 | ||||
chr1:45340388-45340576 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:45500016-45500342 | Common:2; Rare:77; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521878-45522050 | Common:1; Rare:67 | ||||
chr1:45688055-45688237 | Common:1; Rare:52 | ||||
chr1:46303583-46303710 | Common:1; Rare:30 | ||||
chr1:52404467-52404624 | Common:1; Rare:46 | ||||
chr1:54053384-54053687 | Common:5; Rare:96 | ||||
chr1:54200020-54200199 | Rare:35 | ||||
chr1:66924803-66925023 | Rare:94 | ||||
chr1:70205405-70205762 | Rare:132 | ||||
chr1:70354701-70354820 | Rare:41 |